信号序列分离被一个ER应力传感器IRE1α感知到的转位阻塞激活
Ashuei Sogawa1,2, Ryota Komori3,4,5, Kota Yanagitani3,6
1Laboratory of Molecular and Cell Genetics, Graduate School of Biological Sciences, Nara Institute of Science and Technology (NAIST).
Cell structure and function
|September 28, 2023
概括
通过内质网膜 (ER) 中停滞的核糖体堵塞的转位孔触发了信号序列分类,并激活了IRE1α通路. 这种反应旨在重新平衡蛋白质转移到ER.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 蛋白质转移转位 蛋白质转位
背景情况:
- 分泌途径蛋白通过转孔进入内质网膜 (ER).
- 转位子中的核糖体停滞会阻碍蛋白质转位和细胞功能.
研究的目的:
- 为了研究通过停滞的核糖体对哺乳动物细胞的转位子堵塞的影响.
- 了解细胞对受阻的蛋白质转位能力的反应.
主要方法:
- 构建针对ER的转化逮捕蛋白 (ER-TAP) 以诱导转位子堵塞.
- 信号序列 (SS) 选和激活ER应激通路 (IRE1α,PERK) 的分析.
主要成果:
- ER-TAP表达导致了具有高效信号序列的蛋白质的优先转位.
- 转环阻塞特别激活了需要酶1α (IRE1α) 途径的内醇,而不是PERK.
- 激活的IRE1α通路调高了转位元组件,恢复了细胞转位平衡.
结论:
- 跨位子堵塞触发了包括信号序列选择在内的补偿机制.
- IRE1α途径在调整ER转移能力以适应需求方面发挥着至关重要的作用.
- 这种适应性反应使蛋白质的流入与细胞的蛋白质转位能力重新平衡.
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